A glycol dehydration unit includes four subsystems. The glycol contact system, a rich glycol handling system, a rich glycol lifting system and a glycol regeneration system. The rich glycol lifting system lifts the rich glycol from a rich glycol heater to an entry point on a still stahl column and provides for the introduction of stripping gas for the purpose of further removing water from process gas. The glycol dehydration unit uses heretofore undiscovered characteristics of a reboiler and stahl column system.

The methods apparatuses described herein involve recovering of glycol from an aqueous phase to form a stream of recovered glycol and a glycol recovery system. The aqueous phase is fed to the top of a lower theoretical stage in a distillation column. An overhead vapor stream is drawn from the distillation column overhead of an upper theoretical stage, and a bottom stream comprising a stream of regenerated glycol is drawn from the distillation column via a bottom outlet configured below the lower theoretical stage. The stream of recovered glycol comprises the regenerated glycol. In addition, a first middle theoretical stage is situated within the distillation column gravitationally above the lower theoretical stage and below the upper theoretical stage. A side stream of liquid water is drawn from the bottom of the upper theoretical stage in the distillation column.

An acid gas absorbent includes at least one kind of secondary amine compound represented by formula (1): ##STR00001##
where R.sup.1 is a cyclopentyl group or a cyclohexyl group which may be substituted by a substituted or non-substituted alkyl group having 1 to 3 carbon atoms, R.sup.2 and R.sup.3 each indicate an alkylene group having 2 to 4 carbon atoms, and R.sup.2 and R.sup.3 may each be the same or different, and be a straight chain or have a side chain.

The invention concerns a method for treating a hydrocarbon feed gas stream containing at least CO.sub.2 and H.sub.2S to recover a high quality purified CO.sub.2 gas stream, comprising a. Separating said hydrocarbon feed gas stream into a sweetened hydrocarbon gas stream, and an acid gas stream; b. Introducing said gas stream into a Claus unit, c. Introducing the tail gas into a hydrogenation reactor and then into a quench contactor of the Tail Gas Treatment Unit (TGTU); d. Contacting said tail gas stream with a non-selective amine-based solvent into a non-selective acid gas absorption unit of the TGTU; e. Sending the off gas to an incinerator; f. Contacting said enriched gas stream (vii) with a selective H.sub.2S-absorption solvent into a selective H.sub.2S-absorption unit thereby recovering a highly purified CO.sub.2 gas stream and a H.sub.2S-enriched gas stream, as well as the device for carrying said method.

Methods of reducing acid gas from a stream, comprising contacting the stream with a solvent system comprising a glycerol derivative are described herein. Disclosed herein is a composition comprising a glycerol derivative and an acid gas. A method for sweetening a natural gas stream comprising contacting a solvent system comprising a glycerol derivative with a natural gas stream is described herein.

The present disclosure relates to a method for separation of colloidal suspension from a solution of organic compound, wherein the solution of organic compound includes but is not limited to hydrocarbon based solution. More particularly the method provides for removal of colloidal suspension from the solution to obtain clarified hydrocarbon based solution including but not limiting to the compound(s) from the diol family such as mono ethylene glycol (MEG), wherein said removal is achieved by contacting the solution with at least one flocculant followed by chemicals including but not limiting to precipitants. The disclosure also provides a system for carrying out the method of separating colloidal suspension from a solution of organic compound.

A co-axial co-current contactor (CA-CCC) is described herein. The CA-CCC includes an outer annular support ring and an inner annular support ring configured to maintain the CA-CCC within an outer pipe and an inner pipe, respectively. The CA-CCC includes rich liquid flow channels located between the outer annular support ring and the inner annular support ring that are configured to allow a rich liquid stream to flow through the CA-CCC, and a central gas entry cone and gas flow channels configured to allow a gas stream to flow through the CA-CCC. The CA-CCC further includes radial blades configured to secure the central gas entry cone to the inner annular support ring and allow a lean liquid stream to flow into the central gas entry cone and the gas flow channels. The CA-CCC provides for efficient incorporation of liquid droplets formed from the lean liquid stream into the gas stream.

A system for absorbing and separating acid gases may include an absorbing tower in which a gas containing an acid gas is supplied, a recycling tower that is disposed close to the absorbing tower, an absorbent that absorbs an acid gas in the absorbing tower and discharges the acid gas back to the recycling tower while circulating through the absorbing tower and the recycling tower, and a condenser that is connected to the recycling tower and condenses an acid gas produced in the recycling tower, wherein a centrifugal separator that separates the absorbent, using a centrifugal force, is disposed at a lower portion in the absorbing tower.

A lean MEG stream having a first pH level is contacted with a CO.sub.2-rich gas stream to yield a lean MEG product having a second different and lower pH level preferably in a range of 6.5 to 7.0. The system and method can be readily incorporated into a slipstream MEG recovery package, with a source of the lean MEG stream being a MEG regeneration section of the package. The CO.sub.2-rich gas could be a vented CO.sub.2 stream from the MEG reclamation section of the package. Unlike hydrochloric and acetic acid overdosing, CO.sub.2 overdosing of the lean MEG stream does not lead to rapid acidification of the lean MEG product to be stored or injected.

A system and method captures and processes flare gas so that the gas is usable as compressed natural gas (“CNG”). The flare gas is pressurized by a combination of a booster compressor and a CNG compressor. While interstage and between the booster compressor and the CNG compressor, the gas is treated to remove moisture and to separate out higher molecular weight hydrocarbons. The moisture is removed by contacting the interstage gas with a hygroscopic agent within a dehydration unit. The moisture free hydrocarbon fluid is expanded, and/or externally cooled and directed to a knock out drum. Higher molecular weight hydrocarbons are separated from the fluid in the knock out drum. Gas from the knock out drum is compressed in the CNG compressor.